Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H22O2 |
| Molecular Weight | 198.3019 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCCCCCCCC(=O)OC=C
InChI
InChIKey=CMDXMIHZUJPRHG-UHFFFAOYSA-N
InChI=1S/C12H22O2/c1-3-5-6-7-8-9-10-11-12(13)14-4-2/h4H,2-3,5-11H2,1H3
| Molecular Formula | C12H22O2 |
| Molecular Weight | 198.3019 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Regioselective synthesis of kojic acid esters by Bacillus subtilis protease. | 2003 Jun |
|
| Nanoparticles of beta-cyclodextrin esters obtained by self-assembling of biotransesterified beta-cyclodextrins. | 2006 Feb |
|
| Optimization of lipase-catalyzed synthesis of ginsenoside Rb1 esters using response surface methodology. | 2008 Nov 26 |
|
| Regioselective acylation of 3-O-angeloylingenol by Candida antarctica Lipase B. | 2009 Jun |
|
| Lipase nanogel catalyzed transesterification in anhydrous dimethyl sulfoxide. | 2009 Jun 8 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 19:42:23 GMT 2023
by
admin
on
Fri Dec 15 19:42:23 GMT 2023
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| Record UNII |
FF00I399LI
|
| Record Status |
Validated (UNII)
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| Record Version |
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C539564
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225-185-7
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62140
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